Cargando…
Experience-dependent resonance in amygdalo-cortical circuits supports fear memory retrieval following extinction
Learned fear and safety are associated with distinct oscillatory states in the basolateral amygdala (BLA) and medial prefrontal cortex (mPFC). To determine if and how these network states support the retrieval of competing memories, we mimicked endogenous oscillatory activity through optogenetic sti...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459312/ https://www.ncbi.nlm.nih.gov/pubmed/32868768 http://dx.doi.org/10.1038/s41467-020-18199-w |
_version_ | 1783576348035383296 |
---|---|
author | Ozawa, Minagi Davis, Patrick Ni, Jianguang Maguire, Jamie Papouin, Thomas Reijmers, Leon |
author_facet | Ozawa, Minagi Davis, Patrick Ni, Jianguang Maguire, Jamie Papouin, Thomas Reijmers, Leon |
author_sort | Ozawa, Minagi |
collection | PubMed |
description | Learned fear and safety are associated with distinct oscillatory states in the basolateral amygdala (BLA) and medial prefrontal cortex (mPFC). To determine if and how these network states support the retrieval of competing memories, we mimicked endogenous oscillatory activity through optogenetic stimulation of parvalbumin-expressing interneurons in mice during retrieval of contextual fear and extinction memories. We found that exogenously induced 4 Hz and 8 Hz oscillatory activity in the BLA exerts bi-directional control over conditioned freezing behavior in an experience- and context-specific manner, and that these oscillations have an experience-dependent ability to recruit distinct functional neuronal ensembles. At the network level we demonstrate, via simultaneous manipulation of BLA and mPFC, that experience-dependent 4 Hz resonance across BLA-mPFC circuitry supports post-extinction fear memory retrieval. Our findings reveal that post-extinction fear memory retrieval is supported by local and interregional experience-dependent resonance, and suggest novel approaches for interrogation and therapeutic manipulation of acquired fear circuitry. |
format | Online Article Text |
id | pubmed-7459312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74593122020-09-16 Experience-dependent resonance in amygdalo-cortical circuits supports fear memory retrieval following extinction Ozawa, Minagi Davis, Patrick Ni, Jianguang Maguire, Jamie Papouin, Thomas Reijmers, Leon Nat Commun Article Learned fear and safety are associated with distinct oscillatory states in the basolateral amygdala (BLA) and medial prefrontal cortex (mPFC). To determine if and how these network states support the retrieval of competing memories, we mimicked endogenous oscillatory activity through optogenetic stimulation of parvalbumin-expressing interneurons in mice during retrieval of contextual fear and extinction memories. We found that exogenously induced 4 Hz and 8 Hz oscillatory activity in the BLA exerts bi-directional control over conditioned freezing behavior in an experience- and context-specific manner, and that these oscillations have an experience-dependent ability to recruit distinct functional neuronal ensembles. At the network level we demonstrate, via simultaneous manipulation of BLA and mPFC, that experience-dependent 4 Hz resonance across BLA-mPFC circuitry supports post-extinction fear memory retrieval. Our findings reveal that post-extinction fear memory retrieval is supported by local and interregional experience-dependent resonance, and suggest novel approaches for interrogation and therapeutic manipulation of acquired fear circuitry. Nature Publishing Group UK 2020-08-31 /pmc/articles/PMC7459312/ /pubmed/32868768 http://dx.doi.org/10.1038/s41467-020-18199-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ozawa, Minagi Davis, Patrick Ni, Jianguang Maguire, Jamie Papouin, Thomas Reijmers, Leon Experience-dependent resonance in amygdalo-cortical circuits supports fear memory retrieval following extinction |
title | Experience-dependent resonance in amygdalo-cortical circuits supports fear memory retrieval following extinction |
title_full | Experience-dependent resonance in amygdalo-cortical circuits supports fear memory retrieval following extinction |
title_fullStr | Experience-dependent resonance in amygdalo-cortical circuits supports fear memory retrieval following extinction |
title_full_unstemmed | Experience-dependent resonance in amygdalo-cortical circuits supports fear memory retrieval following extinction |
title_short | Experience-dependent resonance in amygdalo-cortical circuits supports fear memory retrieval following extinction |
title_sort | experience-dependent resonance in amygdalo-cortical circuits supports fear memory retrieval following extinction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459312/ https://www.ncbi.nlm.nih.gov/pubmed/32868768 http://dx.doi.org/10.1038/s41467-020-18199-w |
work_keys_str_mv | AT ozawaminagi experiencedependentresonanceinamygdalocorticalcircuitssupportsfearmemoryretrievalfollowingextinction AT davispatrick experiencedependentresonanceinamygdalocorticalcircuitssupportsfearmemoryretrievalfollowingextinction AT nijianguang experiencedependentresonanceinamygdalocorticalcircuitssupportsfearmemoryretrievalfollowingextinction AT maguirejamie experiencedependentresonanceinamygdalocorticalcircuitssupportsfearmemoryretrievalfollowingextinction AT papouinthomas experiencedependentresonanceinamygdalocorticalcircuitssupportsfearmemoryretrievalfollowingextinction AT reijmersleon experiencedependentresonanceinamygdalocorticalcircuitssupportsfearmemoryretrievalfollowingextinction |